2-Ethyl-2-adamantyl methacrylate

2-Ethyl-2-adamantyl methacrylate Basic information
Product Name:2-Ethyl-2-adamantyl methacrylate
Synonyms:2-ethacryloyloxy-2-methyladamantane;2-Ethyl-2-adamantyl methacrylate;2-Ethyl-2-Adamanthyl Methacrylate;2-Ethyladamant-2-yl methacrylate;2-Ethyltricyclo[3.3.1.1~3,7~]dec-2-yl 2-methylprop-2-enoate, EADM;2-Ethyl-2-MethacryloyloxyadaMantane (stabilized with MEHQ);2-Ethyl-2-adamantyl Methacrylate Methacrylic Acid 2-Ethyl-2-adamantyl Ester;2-Ethyl-2-methacryloyloxyadamantane
CAS:209982-56-9
MF:C16H24O2
MW:248.36
EINECS:
Product Categories:
Mol File:209982-56-9.mol
2-Ethyl-2-adamantyl methacrylate Structure
2-Ethyl-2-adamantyl methacrylate Chemical Properties
Melting point 40 °C
Boiling point 318.3±11.0 °C(Predicted)
density 1.04±0.1 g/cm3(Predicted)
storage temp. <0°C
solubility soluble in Methanol
form powder to lump
color White to Almost white
InChIInChI=1S/C16H24O2/c1-4-16(18-15(17)10(2)3)13-6-11-5-12(8-13)9-14(16)7-11/h11-14H,2,4-9H2,1,3H3
InChIKeyDCTVCFJTKSQXED-UHFFFAOYSA-N
SMILESC(OC1(CC)C2CC3CC1CC(C3)C2)(=O)C(C)=C
EPA Substance Registry System2-Propenoic acid, 2-methyl-, 2-ethyltricyclo[3.3.1.13,7]dec-2-yl ester (209982-56-9)
Safety Information
HS Code 2933998090
MSDS Information
2-Ethyl-2-adamantyl methacrylate Usage And Synthesis
Uses2-Ethyl-2-adamantyl methacrylate is a monomer used in the synthesis of organic compounds.
PreparationThe preparation of 2-Ethyl-2-adamantyl methacrylate is as follows:Add 2175ml of n-hexane to the 3L four-necked flask equipped with stirring paddle, condenser tube and thermometer, turn on stirring, add 97g of 2-ethyladamantanol to the system, and slowly add 0.0072g of polymerization inhibitor tetrachlorobenzoquinone to the reaction system , add 72.5g of basic ion exchange resin, adjust pH=7-8, cool down to -10°C, slowly add 72.5g of vinyl methacrylate dropwise to the reaction system, keep the reaction for 6h, monitor the reaction progress, take a sample to detect the reaction is complete After adding 800 ml of water to the reaction system, stirring and extracting the phases, the organic phase was dried, concentrated under reduced pressure and evaporated to dryness to obtain 125 g of 2-ethyl-2-adamantyl methacrylate product with a yield of 93.45%.

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Ethanol Methyl propiolate Ethyl pyruvate Butyl methacrylate Ethyl formate 2-Hydroxyethyl methacrylate Ethylparaben 2-Ethyl-2-adamantyl methacrylate POLYMETHACRYLATE Octadecyl methacrylate ISOXADIFEN-ETHYL Ethyl acetate Ethyl acrylate Methyl acrylate Methyl methacrylate Methacrylic acid Ethyl methacrylate Ethyl cyanoacetate

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